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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013083Generated: October 30, 2026

Acetyl chloride → HCID 57908090, compound

https://huagongshe.com/reaction/1013083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 57908096HCID 57908096—
SolventDichloromethaneHCID 6344—
ProductHCID 57908090HCID 5790809087%

Reaction Steps

tert-Butyl 2-(aminomethyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate (1E) in CH2Cl2 (150 mg, 0.05 M), prepared by the procedure of Example 1, was added Et3N and acetyl chloride at −45° C. The reaction was complete after 20 minutes at −30° C. as determined by LCMS analysis, and then partitioned between ethyl acetate and water. The organics were subsequently washed with NaHCO3 and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was passed thorough a pad of silica to afford the tert-butyl 2-(acetamidomethyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-ene-8-carboxylate (2A, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981904B2
Source datasetuspto-grants-2011_07
ORD IDord-2a219f5a5c5c4080bba29d8b7780f6f5
Source noteuspto-grants-2011_07